Affiliation:
1. Clinic of Medical Department, the First Affiliated Hospital of Xinjiang Medical University, Urumqi 830000, Xinjiang,
China
2. Clinic of Medical Department, the First Affiliated Hospital of Xinjiang Medical University, 830000, Xinjiang,
China
Abstract
Background:
The present study was targeted at investigating the effects of
hsa_circRNA_0008092 (circ_0008092) on hepatocellular carcinoma (HCC) cell proliferation,
migration, invasion and apoptosis, and its related mechanism.
Methods:
The gene expression profiles of GSE166678 were downloaded from the Gene Expression
Omnibus database, and differentially expressed circRNAs in human HCC were screened out.
Besides, circ_0008092, microRNA-502-5p (miR-502-5p) and cyclin D1 (CCND1) expressions in
HCC tissues and cell lines were detected by quantitative real-time polymerase chain reaction (qRTPCR).
Cell countering kit-8 (CCK-8), Transwell and flow cytometry assays were used to detect the
proliferation, migration, invasion and apoptosis of HCC cells. Bioinformatics was utilized to predict
the targeted relationships between miR-502-5p and circ_0008092, as well as miR-502-5p and
CCND1 mRNA 3'-untranslated region (3’UTR). Western blot assay was applied to detect CCND1
protein expression in HCC cells.
Results:
Circ_0008092 was highly expressed in HCC tissues and cells, which was associated with a
shorter survival time in patients with HCC. Circ_0008092 overexpression promoted proliferation,
migration and invasion, and inhibited apoptosis of HCC cells; circ_0008092 knockdown worked
oppositely. Circ_0008092 directly targeted miR-502-5p and negatively modulated miR-502-5p
expression. CCND1 was a target gene of miR-502-5p, and was positively and indirectly modulated
by circ_0008092.
Conclusions:
Our data suggest that circ_0008092 promotes HCC progression by regulating the miR-
502-5p/CCND1 axis.
Publisher
Bentham Science Publishers Ltd.
Subject
Biochemistry,General Medicine,Structural Biology
Cited by
2 articles.
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